메뉴 건너뛰기




Volumn 27, Issue 6, 2002, Pages 477-479

Dyschromatosis universalis hereditaria

Author keywords

[No Author keywords available]

Indexed keywords

MELANIN;

EID: 0036413571     PISSN: 03076938     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2230.2002.01129.x     Document Type: Article
Times cited : (35)

References (10)
  • 1
    • 0034120445 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria: A unique disorder
    • Sethuraman G, Thappa DM, Vijaikumar M et al. Dyschromatosis universalis hereditaria: A unique disorder. Pediatr Dermatol 2000; 17: 70-2.
    • (2000) Pediatr Dermatol , vol.17 , pp. 70-72
    • Sethuraman, G.1    Thappa, D.M.2    Vijaikumar, M.3
  • 2
    • 0017737929 scopus 로고
    • Universal dyschromatosis, small stature and high tone deafness
    • Rycroft RJG, Calnan CD, Wells RS. Universal dyschromatosis, small stature and high tone deafness. Clin Exp Dermatol 1977; 2: 45-8.
    • (1977) Clin Exp Dermatol , vol.2 , pp. 45-48
    • Rycroft, R.J.G.1    Calnan, C.D.2    Wells, R.S.3
  • 3
    • 0021595617 scopus 로고
    • Reticulate pigmentary disorders - A review
    • Griffiths WAD. Reticulate pigmentary disorders - A review. Clin Exp Dermatol 1984; 9: 439-50.
    • (1984) Clin Exp Dermatol , vol.9 , pp. 439-450
    • Griffiths, W.A.D.1
  • 5
    • 0028435303 scopus 로고
    • Dyschromatosis: Its occurrence in two Indian families with unusual feature
    • Gharpuray MB, Tolat SN, Patwardhan SP. Dyschromatosis: Its occurrence in two Indian families with unusual feature. Int J Dermatol 1994; 33: 391-2.
    • (1994) Int J Dermatol , vol.33 , pp. 391-392
    • Gharpuray, M.B.1    Tolat, S.N.2    Patwardhan, S.P.3
  • 6
    • 0031085516 scopus 로고    scopus 로고
    • Dyschromatosis universalis hereditaria: An electron microscopic examination
    • Kim NS, Im S, Kim SC. Dyschromatosis universalis hereditaria: An electron microscopic examination. J Dermatol (Tokyo) 1997; 24: 161-4.
    • (1997) J Dermatol (Tokyo) , vol.24 , pp. 161-164
    • Kim, N.S.1    Im, S.2    Kim, S.C.3
  • 8
    • 0034958530 scopus 로고    scopus 로고
    • One novel and two recurrent missense DKC1 mutations in patients with dyskeratosis congenita (DKC)
    • Heiss NS, Megarbane A, Klauck SM et al. One novel and two recurrent missense DKC1 mutations in patients with dyskeratosis congenita (DKC). Genet Couns 2001; 12: 129-36.
    • (2001) Genet Couns , vol.12 , pp. 129-136
    • Heiss, N.S.1    Megarbane, A.2    Klauck, S.M.3
  • 9
    • 0035960043 scopus 로고    scopus 로고
    • The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita
    • Vutliamy T, Marrone A, Goldman F et al. The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita. Nature 2001; 413: 432-5.
    • (2001) Nature , vol.413 , pp. 432-435
    • Vutliamy, T.1    Marrone, A.2    Goldman, F.3
  • 10
    • 0033781657 scopus 로고    scopus 로고
    • The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21
    • Whittock NV, Coleman CM, McLean WH et al. The gene for Naegeli-Franceschetti-Jadassohn syndrome maps to 17q21. J Invest Dermatol 2000; 115: 694-8.
    • (2000) J Invest Dermatol , vol.115 , pp. 694-698
    • Whittock, N.V.1    Coleman, C.M.2    McLean, W.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.